US9234900B2ActiveUtilityA1

Method for diagnosing glioma and screening for the therapeutics of glioma through identifying protein relocation

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Assignee: AJOU UNIV IND ACAD COOP FOUNDPriority: Apr 22, 2011Filed: Oct 21, 2013Granted: Jan 12, 2016
Est. expiryApr 22, 2031(~4.8 yrs left)· nominal 20-yr term from priority
G01N 33/57557G01N 33/6893G01N 33/57407G01N 2500/00G01N 33/53G01N 33/15G01N 33/68
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Claims

Abstract

The present invention relates to a method for diagnosing glioma by comparing the protein location of an individual to be diagnosed with the normal control nerve cells. More particularly, the present invention relates to a method for diagnosing glioma including determining that an individual has glioma when the expression level of GFRα4 in the endoplasmic reticulum is higher than that in the plasma membrane, and a method for screening a therapeutic agent for glioma. In the diagnostic method of the present invention, the protein expression levels in particular subcellular locations are compared, thereby accurately diagnosing glioma, diagnosing progression of glioma, and predicting prognosis after glioma surgery.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
       1. A method for screening a therapeutic agent for glioma, comprising:
 treating nerve cells with a candidate therapeutic agent for glioma; 
 comparing the GFRα4 relocation from the endoplasmic reticulum to the plasma membrane in said treated nerve cells with GFRα4 relocation from the endoplasmic reticulum to the plasma membrane in a control group that is treated with no candidate therapeutic agent; and identifying a candidate therapeutic agent when said candidate therapeutic agent causes a relocation of GFRα4 from the endoplasmic reticulum to the plasma membrane in said treated nerve cells as compared to said control group. 
 
     
     
       2. A method for screening a therapeutic agent for glioma, comprising:
 treating nerve cells with a candidate therapeutic agent for glioma; and 
 comparing its inhibition of GFRα4 expression in the endoplasmic reticulum with that of the control group that is treated with no candidate therapeutic agent.

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